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Neteera Technologies Ltd

Active in EUDAMED

Israelfrom SRN EUDAMED FDA SRN IL-MF-000043595 FEI 3014739036

Neteera Technologies Ltd is a medical device manufacturer based in Israel, with 4 devices listed in FDA GUDID, FDA 510(k) and EUDAMED (FDA Class II; EU Class IIa) as of 13 Nov 2026.

Devices
4
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 3
  • FDA 510(k) 2
  • EUDAMED 1

A device listed in two registries counts in both.

Device classes
  • FDA Class II 3
  • EU Class IIa 1
Top EMDN categories
Sites and related companies
Identifiers
  • EUDAMED SRN IL-MF-000043595
  • FDA FEI 3014739036
  • DUNS 600710452

At a glance

Counted by deviCERTS from registry records

EU certificates

1 of 1 in force.

See certificates

Market reach

European Union
EUDAMED actor, 1 certificate
United States
FDA FEI
Authorised rep.
MedNet EC-REP GmbHDE

Catalogue4

Newest first, rows 1-4 of 4

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
IL-MF-000043595
FDA FEI number
3014739036
DUNS number
600710452
EU VAT number
515163442
EUDAMED status
Active
EUDAMED registered name
Neteera Technologies Ltd.
EUDAMED abbreviated name
Neteera
Registered address
3, Prof. Rakah St., 9270403, Jerusalem, Israel
Phone
+972 (2) 580-8733
PRRC contact
Yasmin Chen(public in EUDAMED)

EUDAMED certificates1

1 certificate1 valid, 0 expiredMDR 1next expiry 27 Feb 2030

EUDAMED certificates (1)

BSI Group The Netherlands B.V. 2797 1 certificate

  • MDR 810110 Active

    Quality management system EU MDR

    Issued
    28 Feb 2025
    Expires
    27 Feb 2030

Frequently asked questions

How many devices does NETEERA TECHNOLOGIES LTD have in the registry?

The registry currently lists 4 devices for NETEERA TECHNOLOGIES LTD. Devices recorded under merged duplicate company entries are counted once.

Which registries list NETEERA TECHNOLOGIES LTD's devices?

Among its 4 most recently registered devices, NETEERA TECHNOLOGIES LTD has devices listed in EUDAMED (1 device), FDA 510(k) (2 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do NETEERA TECHNOLOGIES LTD's devices fall under?

Among its 4 most recently registered devices, the classes recorded for NETEERA TECHNOLOGIES LTD's devices are Class IIa and Class II. Each device page shows its own class and authorisation.

What EUDAMED certificates are recorded for NETEERA TECHNOLOGIES LTD?

EUDAMED lists 1 certificate for NETEERA TECHNOLOGIES LTD (quality management system) under MDR. 1 is recorded with the status issued. The most recent was issued on 28 Feb 2025.

What are the newest devices from NETEERA TECHNOLOGIES LTD in the registry?

The most recently registered devices listed for NETEERA TECHNOLOGIES LTD include Neteera 130H-Plus 210-00-101-00, Neteera 130H US Kit (DRZ) 130-00-102-00, Neteera 130H/131H Vital Sign Monitoring Sensor and Neteera 130H-Plus.

Generated automatically from registry data and not verified by a human reviewer.